| Primary Device ID | 00763000034375 |
| NIH Device Record Key | 2c423a6d-24a8-4654-b42f-406beb756653 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bojrab |
| Version Model Number | 0507 |
| Company DUNS | 835465063 |
| Company Name | MEDTRONIC XOMED, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000034375 [Primary] |
| ETA | REPLACEMENT, OSSICULAR PROSTHESIS, TOTAL |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-11-15 |
| Device Publish Date | 2021-11-07 |
| 00681490023788 | PROSTHESIS 0507 BOJRAB UNIV 9.0 |
| 00681490023764 | PROSTHESIS 0506 BOJRAB UNIVERSAL 7MM |
| 00681490017572 | PROSTHESIS 0308 BOJRAB UNIV H/A OFFSET |
| 00681490017565 | PROSTHESIS 0306 BOJRAB UNIV HA 7MM |
| 00721902817427 | PROSTHESIS 0385 BOJRAB UNIV POLYCEL |
| 00763000036508 | PROSTHESIS 0385 BOJRAB UNIV POLYCEL |
| 00763000034375 | PROSTHESIS 0507 BOJRAB UNIV 9.0 |
| 00763000034368 | PROSTHESIS 0506 BOJRAB UNIVERSAL 7MM |
| 00763000034221 | PROSTHESIS 0308 BOJRAB UNIV H/A OFFSET |
| 00763000034214 | PROSTHESIS 0306 BOJRAB UNIV HA 7MM |
| 00763000913496 | PROSTHESIS 0506 BOJRAB UNIVERSAL 7MM |